54 results match your criteria: "Stanford University of Medicine[Affiliation]"

Hsp90 Promotes Gastric Cancer Cell Metastasis and Stemness by Regulating the Regional Distribution of Glycolysis-Related Metabolic Enzymes in the Cytoplasm.

Adv Sci (Weinh)

September 2024

State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.

Heat-shock protein 90 (Hsp90) plays a crucial role in tumorigenesis and tumor progression; however, its mechanism of action in gastric cancer (GC) remains unclear. Here, the role of Hsp90 in GC metabolism is the focus of this research. High expression of Hsp90 in GC tissues can interact with glycolysis, collectively affecting prognosis in clinical samples.

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Immune checkpoint inhibitor-mediated colitis (IMC) is a common adverse event of treatment with immune checkpoint inhibitors (ICI). We hypothesize that genetic susceptibility to Crohn's disease (CD) and ulcerative colitis (UC) predisposes to IMC. In this study, we first develop a polygenic risk scores for CD (PRS) and UC (PRS) in cancer-free individuals and then test these PRSs on IMC in a cohort of 1316 patients with ICI-treated non-small cell lung cancer and perform a replication in 873 ICI-treated pan-cancer patients.

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Multiple sclerosis (MS) is an autoimmune disease characterized by demyelination of the central nervous system (CNS). Autologous hematopoietic cell transplantation (HCT) shows promising benefits for relapsing-remitting MS in open-label clinical studies, but the cellular mechanisms underlying its therapeutic effects remain unclear. Using single-nucleus RNA sequencing, we identify a reactive myeloid cell state in chronic experimental autoimmune encephalitis (EAE) associated with neuroprotection and immune suppression.

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Background: Disparities in pediatric heart transplant outcomes based on socioeconomic status (SES) have been previously observed. However, there is a need to reevaluate these associations in contemporary settings with advancements in transplant therapies and increased awareness of health disparities. This retrospective study aims to investigate the relationship between SES and outcomes for pediatric heart transplant patients.

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Article Synopsis
  • Immune checkpoint inhibitors (ICIs) have vastly improved cancer treatment but can lead to serious immune-related adverse events (irAEs), particularly immune checkpoint inhibitor-mediated colitis (IMC), which can mimic diseases like Crohn's and ulcerative colitis.
  • Researchers hypothesized that genetic predispositions related to these diseases might increase the risk of developing IMC in cancer patients receiving ICIs, and they developed polygenic risk scores (PRS) to test this in a study of 1,316 non-small cell lung cancer patients.
  • The study found that higher PRS scores were linked to an increased risk of all-grade and severe IMC, suggesting that genetic testing could help identify patients at higher risk and enable better monitoring and
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Augmentation of a neuroprotective myeloid state by hematopoietic cell transplantation.

bioRxiv

March 2023

Institute for Stem Cell Biology and Regenerative Medicine and Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Multiple sclerosis (MS) is an autoimmune disease associated with inflammatory demyelination in the central nervous system (CNS). Autologous hematopoietic cell transplantation (HCT) is under investigation as a promising therapy for treatment-refractory MS. Here we identify a reactive myeloid state in chronic experimental autoimmune encephalitis (EAE) mice and MS patients that is surprisingly associated with neuroprotection and immune suppression.

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Calcineurin (Cn), a phosphatase important for synaptic plasticity and neuronal development, has been implicated in the etiology and pathophysiology of neuropsychiatric disorders, including schizophrenia, intellectual disability, autism spectrum disorders, epilepsy, and Alzheimer's disease. Forebrain-specific conditional Cn knockout mice have been known to exhibit multiple behavioral phenotypes related to these disorders. In this study, we investigated whether Cn mutant mice show pseudo-immaturity of the dentate gyrus (iDG) in the hippocampus, which we have proposed as an endophenotype shared by these disorders.

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Purpose: Brain metastasis is common in lung cancer, and treatment of brain metastasis can lead to significant morbidity. Although early detection of brain metastasis may improve outcomes, there are no prediction models to identify high-risk patients for brain magnetic resonance imaging (MRI) surveillance. Our goal is to develop a machine learning-based clinicogenomic prediction model to estimate patient-level brain metastasis risk.

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Article Synopsis
  • This study investigates the differences by sex in patients with Pediatric Acute-onset Neuropsychiatric Syndrome (PANS), examining clinical characteristics, treatment, and psychosocial factors among 205 patients, with 87 females and 118 males.
  • Results showed that males had higher aggression scores compared to females, as measured by the Modified Overt Aggression Scale (MOAS), and generally received immunotherapy treatment sooner despite no significant differences in age of onset or overall impairment levels between sexes.
  • While males exhibited more aggressive behavior, both sexes experienced similar overall functioning impairments, suggesting that sex may influence treatment decisions without affecting overall disease severity.
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Background: Posttraumatic stress disorder (PTSD) is associated with markers of accelerated aging. Estimates of brain age, compared to chronological age, may clarify the effects of PTSD on the brain and may inform treatment approaches targeting the neurobiology of aging in the context of PTSD.

Method: Adult subjects (N = 2229; 56.

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Article Synopsis
  • Sympathetic activation can trigger dangerous heart issues in patients with long QT syndrome type 1 (LQT1), which is caused by certain genetic mutations.
  • Researchers studied sympathetic neurons derived from human stem cells of LQT1 patients to understand their functional characteristics, focusing on abnormalities linked to cardiac arrhythmias.
  • The results showed that these LQT1 neurons exhibited hyperactivity with increased neurotransmitter release and action potentials compared to healthy neurons, indicating that these neuronal changes may contribute to the arrhythmogenic risk in LQT1.
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Impact of Low-Dose Computed Tomography Screening for Primary Lung Cancer on Subsequent Risk of Brain Metastasis.

J Thorac Oncol

September 2021

Quantitative Sciences Unit, Department of Medicine, Stanford University School of Medicine, Stanford, California; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California; Department of Neurosurgery, Stanford University School of Medicine, Stanford, California. Electronic address:

Introduction: Brain metastasis (BM) is one of the most common metastases from primary lung cancer (PLC). Recently, the National Lung Screening Trial revealed the efficacy of low-dose computed tomography (LDCT) screening on LC mortality reduction. Nevertheless, it remains unknown if early detection of PLC through LDCT may be potentially beneficial in reducing the risk of subsequent metastases.

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Cost Structures of US Organ Procurement Organizations.

Transplantation

December 2021

Abdominal Transplantation, Department of Surgery, University of California, San Francisco, San Francisco, CA.

Background: The goal is to provide a national analysis of organ procurement organization (OPO) costs.

Methods: Five years of data, for 51 of the 58 OPOs (2013-2017, a near census) were obtained under a FOIA. OPOs are not-for-profit federal contractors with a geographic monopoly.

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Article Synopsis
  • Maternal X chromosome abnormalities can lead to conflicting results between noninvasive prenatal tests and definitive evaluations, potentially causing unnecessary invasive procedures, so early diagnosis is crucial.
  • The study sought to validate a noninvasive prenatal test based on single nucleotide polymorphisms to detect maternal-origin X chromosome abnormalities.
  • Results showed a high confirmation rate of suspected maternal X chromosome abnormalities in a significant portion of cases, particularly for Turner syndrome and 47,XXX, highlighting the effectiveness of the new noninvasive testing approach.
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Background: The current article is a short review of an Alimera Sciences-sponsored symposium held during The 15th International Ocular Inflammation Society Congress in Taiwan on the 14th November 2019 entitled, 'Preventing relapse of non-infectious uveitis effecting the posterior segment of the eye - evaluating the 0.2 μg/day fluocinolone acetonide intravitreal implant.'

Main Text: The fluocinolone acetonide intravitreal implant was approved in Europe for the prevention of relapse in recurrent non-infectious uveitis affecting the posterior segment of the eye and offers a systemic therapy-sparing treatment option by providing low daily dose of corticosteroid into the vitreous for up to 3 years.

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  • Dendritic cells (DCs) are crucial antigen-presenting cells that can drive either proinflammatory or tolerogenic immune responses depending on their origin and interactions with other immune cells.
  • A study reveals a novel pathway where monocytes, when cultured with regulatory T cells (Tregs) and T helper cells (Th), differentiate into regulatory DCs that can promote the formation of Tregs from naïve T cells.
  • The differentiation process relies on direct cell contact and specific cytokines, particularly highlighting the importance of IL-10, and could play a significant role in maintaining immune tolerance in environments rich in Tregs, like tumors.
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Caregivers' impression of epilepsy surgery in patients with tuberous sclerosis complex.

Epilepsy Behav

October 2020

Department of Neurology, Stanford University of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA.

Epilepsy surgery is successful in the majority of patients with tuberous sclerosis complex (TSC), with high rates of postoperative seizure reduction and even seizure freedom. Epilepsy surgery is recommended after failing two appropriate antiseizure medication trials; however, this is rare in clinical practice. We hypothesized that following surgery, caregivers' perspectives on the path they took to epilepsy surgery would inform changes in clinical practice and future research to increase utilization and early use of surgery.

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Circulating levels of adiponectin, an adipocyte-secreted protein associated with cardiovascular and metabolic risk, are highly heritable. To gain insights into the biology that regulates adiponectin levels, we performed an exome array meta-analysis of 265,780 genetic variants in 67,739 individuals of European, Hispanic, African American, and East Asian ancestry. We identified 20 loci associated with adiponectin, including 11 that had been reported previously (p < 2 × 10).

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As part of a longitudinal investigation on implementation of 2 evidence-based psychotherapies (EBPs) for posttraumatic stress disorder, psychotherapists from 38 Department of Veterans Affairs residential treatment programs across the United States were asked to complete reflective journals every 4 months for a 1-year time period in regard to their successes and challenges in using prolonged exposure and cognitive processing therapy. This paper provides content analysis on the reflective journals of 24 of these providers. Five main themes were identified: EBPs are great but not sufficient for patients in residential treatment with chronic posttraumatic stress disorder and complicated life circumstances, and thus, more treatment is necessary after discharge.

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Objectives: Assessing late-life anxiety using an instrument with sound psychometric properties including cross-cultural invariance is essential for cross-national aging research and clinical assessment. To date, no cross-national research studies have examined the psychometric properties of the frequently used Geriatric Anxiety Inventory (GAI) in depth.

Method: Using data from 3,731 older adults from 10 national samples (Australia, Brazil, Canada, The Netherlands, Norway, Portugal, Spain, Singapore, Thailand, and United States), this study used bifactor modeling to analyze the dimensionality of the GAI.

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Importance: Electronic health record (EHR) biobanks containing clinical and genomic data on large numbers of individuals have great potential to inform drug discovery. Individuals with interleukin 6 receptor (IL6R) single-nucleotide polymorphisms (SNPs) who are not receiving IL6R blocking therapy have biomarker profiles similar to those treated with IL6R blockers. This gene-drug pair provides an example to test whether associations of IL6R SNPs with a broad range of phenotypes can inform which diseases may benefit from treatment with IL6R blockade.

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Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

Diabetologia

October 2018

Department of Medical Sciences, Molecular Epidemiology, Uppsala University, EpiHubben, MTC-huset, 751 85, Uppsala, Sweden.

Aims/hypothesis: Coronary artery disease (CAD) is a common complication among individuals with diabetes. A better understanding of the genetic background of CAD in this population has the potential to suggest novel molecular targets for screening, risk assessment and drug development.

Methods: We performed a genome-wide association study of CAD in 15,666 unrelated individuals (3,968 CAD cases and 11,698 controls) of white British ancestry with diabetes at inclusion in the UK Biobank study.

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The 14th International Workshops on Opportunistic Protists (IWOP-14) was held August 10-12, 2017 in Cincinnati, OH, USA. The IWOP meetings focus on opportunistic protists (OIs); for example, free-living amoebae, Pneumocystis spp., Cryptosporidium spp.

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Flow cytometry analysis of T-cell subsets in cerebrospinal fluid of narcolepsy type 1 patients with long-lasting disease.

Sleep Med

April 2018

Department of Biomedical and Neuromotor Sciences (DIBINEM), University of Bologna, Bologna, Italy; IRCCS Istituto delle Scienze Neurologiche, Bologna, Italy. Electronic address:

Background: Type 1 narcolepsy (NT1) is a central hypersomnia linked to the destruction of hypocretin-producing neurons. A great body of genetic and epidemiological data points to likely autoimmune disease aetiology. Recent reports have characterized peripheral blood T-cell subsets in NT1, whereas data regarding the cerebrospinal fluid (CSF) immune cell composition are lacking.

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Foxp3 regulatory T cells maintain the bone marrow microenvironment for B cell lymphopoiesis.

Nat Commun

May 2017

Department of Medicine, Division of Blood and Marrow Transplantation, Stanford University, 269W. Campus Drive, Stanford, California 94305, USA.

Foxp3 regulatory T cells (Treg cells) modulate the immune system and maintain self-tolerance, but whether they affect haematopoiesis or haematopoietic stem cell (HSC)-mediated reconstitution after transplantation is unclear. Here we show that B-cell lymphopoiesis is impaired in Treg-depleted mice, yet this reduced B-cell lymphopoiesis is rescued by adoptive transfer of affected HSCs or bone marrow cells into Treg-competent recipients. B-cell reconstitution is abrogated in both syngeneic and allogeneic transplantation using Treg-depleted mice as recipients.

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